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  2. Schumann resonances - Wikipedia

    en.wikipedia.org/wiki/Schumann_resonances

    The global electromagnetic resonance phenomenon is named after physicist Winfried Otto Schumann who predicted it mathematically in 1952. Schumann resonances are the principal background in the part of the electromagnetic spectrum [2] from 3 Hz through 60 Hz [3] and appear as distinct peaks at extremely low frequencies around 7.83 Hz (fundamental), 14.3, 20.8, 27.3, and 33.8 Hz.

  3. Mesomeric effect - Wikipedia

    en.wikipedia.org/wiki/Mesomeric_effect

    The +M effect, also known as the positive mesomeric effect, occurs when the substituent is an electron donating group. The group must have one of two things: a lone pair of electrons, or a negative charge. In the +M effect, the pi electrons are transferred from the group towards the conjugate system, increasing the density of the system.

  4. Molecular vibration - Wikipedia

    en.wikipedia.org/wiki/Molecular_vibration

    A molecular vibration is a periodic motion of the atoms of a molecule relative to each other, such that the center of mass of the molecule remains unchanged. The typical vibrational frequencies range from less than 10 13 Hz to approximately 10 14 Hz, corresponding to wavenumbers of approximately 300 to 3000 cm −1 and wavelengths of approximately 30 to 3 μm.

  5. Triple-alpha process - Wikipedia

    en.wikipedia.org/wiki/Triple-alpha_process

    It was instead astrophysicist Fred Hoyle who, in 1953, used the abundance of carbon-12 in the universe as evidence for the existence of a carbon-12 resonance. The only way Hoyle could find that would produce an abundance of both carbon and oxygen was through a triple-alpha process with a carbon-12 resonance near 7.68 MeV, which would also ...

  6. Resonance (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Resonance_(chemistry)

    The resonance proposal also helped explain the number of isomers of benzene derivatives. For example, Kekulé's structure would predict four dibromobenzene isomers, including two ortho isomers with the brominated carbon atoms joined by either a single or a double bond. In reality there are only three dibromobenzene isomers and only one is ortho ...

  7. Inductive effect - Wikipedia

    en.wikipedia.org/wiki/Inductive_effect

    In benzoic acid, the carbon atoms which are present in the ring are sp 2 hybridised. As a result, benzoic acid ( pK a =4.20 ) is a stronger acid than cyclohexanecarboxylic acid ( pK a =4.87 ). Also, in aromatic carboxylic acids, electron-withdrawing groups substituted at the ortho and para positions can enhance the acid strength.

  8. Nuclear Overhauser effect - Wikipedia

    en.wikipedia.org/wiki/Nuclear_Overhauser_effect

    A phenomenological definition of the NOE in nuclear magnetic resonance spectroscopy (NMR) is the change in the integrated intensity (positive or negative) of one NMR resonance that occurs when another is saturated by irradiation with an RF field. The change in resonance intensity of a nucleus is a consequence of the nucleus being close in space ...

  9. Resonance (particle physics) - Wikipedia

    en.wikipedia.org/wiki/Resonance_(particle_physics)

    Thus, the lifetime of a particle is the direct inverse of the particle's resonance width. For example, the charged pion has the second-longest lifetime of any meson, at 2.6033 × 10 −8 s. [2] Therefore, its resonance width is very small, about 2.528 × 10 −8 eV or about 6.11 MHz. Pions are generally not considered as "resonances".

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